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1.
Saudi Med J ; 27(8): 1161-6, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16883445

ABSTRACT

OBJECTIVE: To investigate the relationship between some thrombophilic parameters and pregnancy induced hypertension (PIH). METHODS: The study took place at the Department of Obstetrics and Gynecology, Perinatology Unit, Faculty of Medicine, Cukurova University, Turkey, between January 2002 and December 2002. We evaluated 202 patients. Patients were divided into 2 groups: control group comprised 102 normotensive patients >20 weeks of pregnancy without any medical or pregnancy related pathologies and the study group comprised 100 patients over 20 weeks of pregnancy with PIH. These hypertensive patients were divided into 6 sub-groups as follows: eclampsia, severe preeclampsia, preeclampsia, chronic hypertension plus superimposed preeclampsia, eclampsia, and hemolysis elevated liver enzymes and thrombocytopenia (HELLP) syndrome. RESULTS: In all cases, complete blood count, antithrombin III, protein S levels, factor V Leiden mutation, prothrombin 20210 mutation, methylenetetrahydrofolate reductase (MTHFR) 677 mutation and homocysteine levels were studied. Statistical analysis of the data was carried out using SPSS version 11.0 program. In comparing the 2 groups we used Mann-Whitney U tests. In comparing the PIH subgroups we used Kruskal-Wallis tests. The levels of p<0.05 were accepted as statistically significant. CONCLUSION: Antithrombin III deficiency, protein C deficiency, hyperhomocysteinanemia were found to be associated with PIH groups. But protein S deficiency, and homozygote factor V Leiden mutation, prothrombin 20210, MTHFR 677 mutation were not found to be related with PIH.


Subject(s)
Eclampsia/diagnosis , HELLP Syndrome/diagnosis , Pre-Eclampsia/diagnosis , Thrombophilia/congenital , Thrombophilia/diagnosis , Antithrombin III Deficiency/genetics , Female , Humans , Hyperhomocysteinemia/genetics , Hypertension, Pregnancy-Induced/diagnosis , Pregnancy , Protein C Deficiency/genetics , Thrombophilia/genetics , Turkey
2.
Eur Neuropsychopharmacol ; 16(4): 241-7, 2006 May.
Article in English | MEDLINE | ID: mdl-16176870

ABSTRACT

In the present study, the effects of N-methyl-D-aspartate (NMDA) receptor antagonist, D,L-2-amino-5-phosphonopentanoic acid (AP5) bilaterally infused into the dorsal hippocampus (2.0 microl /5 microg), on the retrieval of fear memory to partial and whole foreground cues were evaluated by using a step-through passive avoidance and Pavlovian fear conditioning. In the both conditioning tasks, following a 30-s preshock exposure period to the shock-associated context, rats received a single shock in a foreground manner for fear memory exhibition by freezing. Rats with AP5 infusion 5 min before the retrieval tests showed profound freezing deficits either immediately or 48 h after the shock in the testing section of the passive avoidance chamber where foreground cues was partially presented. In the Pavlovian conditioning chamber where fear conditioning was tested in the whole of the context that was explicitly paired with the shock, AP5 rats in all infusion schedules exhibited robust freezing responses. These results showed that hypofunction of the hippocampal NMDA receptors impaired the retrieval of fear memory to partial, and not whole, foreground cues. This suggests that NMDA receptors of the hippocampus are involved in the formation of background context representations about foreground events when there is a deficit in perceiving certain sensory properties of the foreground retrieval cues.


Subject(s)
Conditioning, Classical/physiology , Fear , Hippocampus/physiopathology , Memory Disorders/physiopathology , Receptors, N-Methyl-D-Aspartate/physiology , 2-Amino-5-phosphonovalerate/pharmacology , Analysis of Variance , Animals , Behavior, Animal , Conditioning, Classical/drug effects , Dose-Response Relationship, Drug , Electroshock/adverse effects , Excitatory Amino Acid Antagonists/pharmacology , Freezing Reaction, Cataleptic/drug effects , Hippocampus/drug effects , Male , Memory Disorders/chemically induced , Rats , Rats, Wistar , Time Factors
3.
Int J Neurosci ; 113(8): 1023-42, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12888418

ABSTRACT

Paw preference and paw frequency was studied in female rats. Paw preference was assessed using a modified version of food reaching task in quadrupedal position. Of 68 rats, 56 (82.4%) were right-handed, 7 (10.3%) were left-handed, and 5 (7.4%) were mixed-handed. There were significantly more right-handers than left-handers. The distribution of right minus left (L) paw reach (R + L = 50) was not U-shaped, it was J-shaped like in humans. Estrus cycle was a significant factor influencing the right-paw entry scores: most of left-handers were in estrus and proestrus, most of left -handers were in estrus, and most of mixed-handers were in postestrus. In right- and non-right- handers, the frequency of right-paw usage (right-hand skill) increased linearly with testing days, but the frequency of left-hand usage (left-hand skill) did not show significant changes with the successive testing days. Controlling for body weight and estrus only accentuated these results. It was concluded that distribution of hand preference in rats is J-shaped and there is a right-sided population bias in handedness in rats like in humans. The results suggested that motor learning in paw skill is mainly involved the left brain in right- and mixed-handed rats, not the right brain: only the left brain has the inbuilt capacity for motor learning in female rats. Such an asymmetric cognitive control in an animal model may have a major impact in many aspects of biology in respect to normal functioning, superior talents, and disease (see Geschwind, 1985).


Subject(s)
Brain/physiology , Functional Laterality/physiology , Psychomotor Performance/physiology , Upper Extremity/physiology , Animals , Estrous Cycle/physiology , Female , Rats , Rats, Wistar
4.
Int J Neurosci ; 112(5): 525-35, 2002 May.
Article in English | MEDLINE | ID: mdl-12325388

ABSTRACT

The aim of the present study was to investigate the effects of excitotoxic damage of the serotonergic cell bodies in the median raphe nucleus (MRN) on the scopolamine-induced working memory deficits in a single-trial light/dark inhibitory avoidance task. Rats were given 1 mg/kg of scopolamine hydrobromide (intraperitonal, i.p.) or saline before the inhibitory avoidance training, in which initial preference to the dark compartment (escape latency) was used to measure nonmnemonic behaviors, and response latency to enter the dark compartment immediately after the shock was used to measure working memory. It was found that scopolamine significantly reduced escape latencies in sham-lesioned rats, whereas it had no effect in the rats with MRN lesions. Although MRN lesion per se did not alter response latency, it prevented scopolamine-induced decrease in this parameter. These results suggest that the antagonistic interactive processes between serotonergic projections of the MRN and the muscarinic cholinergic system modulate nonmnemonic attentional component of working memory formation in the inhibitory avoidance.


Subject(s)
Avoidance Learning , Memory , Muscarinic Antagonists , Raphe Nuclei/metabolism , Raphe Nuclei/pathology , Scopolamine , Alzheimer Disease/chemically induced , Alzheimer Disease/pathology , Alzheimer Disease/psychology , Animals , Behavior, Animal , Excitatory Amino Acid Agonists , Ibotenic Acid , Male , Rats , Rats, Wistar , Reaction Time , Serotonin/metabolism
5.
Brain Res Bull ; 57(5): 683-8, 2002 Mar 15.
Article in English | MEDLINE | ID: mdl-11927373

ABSTRACT

The experiments investigated the interactions between median raphe nucleus (MRN) serotonergic and septo-hippocampal muscarinic cholinergic systems in the modulation of forming and storing performances of working memory. Rats with ibotenic acid-induced MRN-lesion bilaterally received scopolamine (2-4 microg/each side) infusion into the dentate gyrus of the dorsal hippocampus and were tested in a single trial step-through inhibitory avoidance. Initial preference to the dark compartment (escape latency) was taken as the measure of non-mnemonic behaviours and response latency to enter the dark compartment immediately after the foot-shock was used to measure working memory. The high-dose scopolamine infusion 10 min before the training decreased escape latencies in the sham-lesioned rats, whereas had no effect in the MRN-lesioned rats. Although MRN lesion per se did not alter response latency, it alleviated pre-training scopolamine-induced decrease, but aggravated post-training scopolamine-induced reduction in this parameter. These results suggest that the antagonistic interactive processes between MRN-serotonergic and hippocampal cholinergic systems modulate non-mnemonic component of working memory formation, whereas the storing performance of working memory is modulated by the synergistic interactions between these systems in the hippocampus, mainly in the dentate gyrus.


Subject(s)
Cholinergic Fibers/drug effects , Fornix, Brain/drug effects , Hippocampus/drug effects , Memory, Short-Term/drug effects , Neural Inhibition/drug effects , Pons/physiopathology , Raphe Nuclei/physiopathology , Receptors, Muscarinic/drug effects , Septal Nuclei/drug effects , Serotonin/metabolism , Animals , Avoidance Learning/drug effects , Avoidance Learning/physiology , Cholinergic Fibers/metabolism , Dose-Response Relationship, Drug , Fornix, Brain/metabolism , Fornix, Brain/physiopathology , Hippocampus/metabolism , Hippocampus/physiopathology , Ibotenic Acid/pharmacology , Male , Memory, Short-Term/physiology , Muscarinic Antagonists/pharmacology , Neural Inhibition/physiology , Neurons/cytology , Neurons/drug effects , Neurons/metabolism , Neurotoxins/pharmacology , Pons/drug effects , Pons/injuries , Raphe Nuclei/drug effects , Raphe Nuclei/injuries , Rats , Rats, Wistar , Reaction Time/drug effects , Reaction Time/physiology , Receptors, Muscarinic/metabolism , Scopolamine/pharmacology , Septal Nuclei/metabolism , Septal Nuclei/physiopathology , Synaptic Transmission/drug effects , Synaptic Transmission/physiology
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